US4613657A - Method for anionic homopolymerization of α-trifluoromethylacrylate - Google Patents
Method for anionic homopolymerization of α-trifluoromethylacrylate Download PDFInfo
- Publication number
- US4613657A US4613657A US06/826,585 US82658586A US4613657A US 4613657 A US4613657 A US 4613657A US 82658586 A US82658586 A US 82658586A US 4613657 A US4613657 A US 4613657A
- Authority
- US
- United States
- Prior art keywords
- trifluoromethylacrylate
- polymer
- alkyl group
- butoxide
- group
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F120/00—Homopolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F120/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F120/10—Esters
- C08F120/22—Esters containing halogen
- C08F120/24—Esters containing halogen containing perhaloalkyl radicals
Definitions
- This invention relates to a method of anionically homopolymerizing an ⁇ -trifluoromethylacrylate to obtain a methanol-insoluble polymer.
- Fluorine-containing acrylic or methacrylic esters provide industrially important functional polymers.
- fluorine-containing acrylic or methacrylic polymers In view of some properties unique to fluorine-containing polymers, such as excellent resistance to chemicals, water- and oil-repelling property and suitably low indices of refraction, extensive studies have been conducted on the uses of fluorine-containing acrylic or methacrylic polymers as or in, for example, paint materials, textile oil, plastic optical materials for optical fibers and other elements of optical circuits, contact lenses, dental materials and resist materials. Some items have already been developed to the stage of practical applications. Polymers of this category are acquiring greater importance as the needs for new functional materials are increasing in various fields of advanced technology.
- the aforementioned polymers were mostly of fluorine-containing acrylic or methacrylic esters represented by the general formula (A): ##STR1## wherein R is hydrogen atom or methyl group and R' is a fluorinated alkyl group. That is, fluorine atoms were introduced exclusively into the ester radical part of the monomer.
- methyl ⁇ -fluoroacrylate can be homopolymerized at good yields by using a radical polymerization initiator, and can also be copolymerized with methyl methacrylate.
- ⁇ -trifluoromethylacrylates are somewhat different in polymerizability from other fluorine-containing acrylic and methacrylic esters.
- homopolymerization of an ⁇ -trifluoromethylacrylate can be accomplished only by anionic polymerization, and the yield of the homopolymer is very low when a popular anionic polymerization catalyst such as n-butyllithium or Grignard reagent is used.
- a popular anionic polymerization catalyst such as n-butyllithium or Grignard reagent
- the yield of the polymer is improved to some extent by using pyridine as the catalyst, the obtained polymer consists of a methanol-soluble fraction and a methanol-insuluble fraction. That is, there is no industrially practicable method for anionic homopolymerization of ⁇ -trifluoromethylacrylates.
- this invention provides a method of preparing a homopolymer of an ⁇ -trifluoromethylacrylate represented by the general formula (1), the method comprising the step of keeping the monomer of the ⁇ -trifluoromethylacrylate dissolved in an organic solvent in the presence of an anionic polymerization catalyst which is an alkoxide represented by the general formula (2): ##STR2## wherein R represents an alkyl group or a fluorine-containing alkyl group:
- R' represents an alkyl group and M represents an alkali metal.
- the alkali metal M may be any of Li, Na, K, Rb and Cs. In practice, however, it is suitable to make a selection among lithium, sodium and potassium alkoxides, and it is preferable that the alkyl group R' in the alkoxide has from 1 to 4 carbon atom(s).
- the ⁇ -trifluoromethylacrylate monomer may contain fluorine atom(s) in the ester radical too.
- fluorine atom(s) in the ester radical too.
- An example of such cases is 2,2,2-trifluoroethyl ⁇ -trifluoromethylacrylate.
- the anionic homopolymerization according to the invention is carried out in the manner of solution polymerization.
- the polymer may or may not dissolve in the solvent.
- the solution after the reaction is poured into a suitable liquid to cause complete precipitation of the polymer.
- the anionic polymerization reaction must be performed in the absence of water and elemental or molecular oxygen.
- the polymerization reaction temperature is variable over the range of from about -78° C. to about 100° C. depending on the reaction materials.
- homopolymers of ⁇ -trifluoromethylacrylates obtained by the method according to the invention are insoluble in methanol. These polymers are promising as high functional resins useful in various fields including paint materials. resist materials and plastic optical materials.
- ⁇ -Trifluoromethylacrylates that can be homopolymerized by the method according to the invention include esters of ⁇ -trifluoromethylacrylic acid with an aliphatic alcohol, such as methyl ⁇ -trifluoromethyl acrylate, ethyl ⁇ -trifluoromethylacrylate, n-propyl ⁇ -trifluoromethylacrylate, isopropyl ⁇ -trifluoromethylacrylate, n-butyl ⁇ -trifluoromethylacrylate, t-butyl ⁇ -trifluoromethylacrylate and 2-ethylhexyl ⁇ -trifluoromethylacrylate, and esters of ⁇ -trifluoromethylacrylic acid with a fluorinated alcohol, such as 2,2,2-trifluoroethyl ⁇ -trifluoromethylacrylate, 1H,1H-heptafluorobutyl ⁇ -trifluoromethylacrylate, 1H,1H,7H-dodeca
- the anionic polymerization reaction according to the invention must be carried out in an organic solvent which is practically free of water and elemental or molecular oxygen. It is suitable to use an inactive aprotic solvent which can be selected from aliphatic and aromatic hydrocarbons such as n-hexane, n-heptane, benzene, toluene and xylene and also from some ethers such as ethyl ether, di-n-butyl ether, tetrahydrofuran and dioxane.
- the selected solvent is dehydrated, degassed and refined by distillation.
- the quantity of the solvent per unit quantity of the reactant is not strictly limited.
- An alkali metal alkoxide is chosen as the anionic polymerization catalyst.
- Typical examples of useful alkali metal alkoxides are lithium methoxide, sodium methoxide, potassium methoxide, lithium ethoxide, sodium ethoxide, potassium ethoxide, lithium n-propoxide.
- the amount of the anionic polymerization catalyst is not necessarily limited. However, it is preferable that the catalyst amounts to 0.01-5 mol % of the ⁇ -trifluoromethylacrylate monomer.
- the reactor to carry out the polymerization reaction may be of any type.
- an ampule-like glass reactor or an ordinary solution polymerization reactor provided with a stirrer can be used. It is necessary to dry out the interior of the reactor and to purge oxygen-containing gases from the reactor before charging the reaction materials into the reactor.
- the reaction temperature for the polymerization ranges from about -78° C. to about 100° C. In general a very Suitable reaction temperature can be found within the range from -50° C. to 80° C.
- the polymer formed by a reaction according to the invention After separating the polymer formed by a reaction according to the invention from the mother liquor or from the liquid used for precipitation, the polymer is washed first with dilute hydrochloric acid and then with water, followed by drying.
- Ethyl ⁇ -trifluoromethylacrylate monomer (b.p. 103°-105° C.) was refined by reflux distillation in the presence of calcium hydride. Together with 50 ml of toluene and 0.08 g (0.001 mol) of lithium t-butoxide, 8.4 g (0.05 mol) of refined ethyl ⁇ -trifluoromethylacrylate monomer was put into a glass ampule. After replacing the gas atmosphere in the ampule by nitrogen gas, the ampule was sealed and was left standing at -20° C. for 7 days to allow polymerization of the ⁇ -fluoromethylacrylate. The obtained polymer was washed first with dilute hydrochloric acid and then with water, and was dried under vacuum. The yield of the polymer was 100%.
- the polymer was insoluble in methanol, but it was soluble in any of tetrahydrofuran, chloroform and benzene.
- Example 2 Using the same method and apparatus as in Example 1, 14.5 g (0.05 mol) of hexafluoroisopropyl ⁇ -trifluoromethylacrylate was mixed with 50 ml of toluene and 0.08 g (0.001 mol) of lithium t-butoxide and was subjected to polymerization at -20° C. for 7 days. The yield of the polymer was 68%. This polymer was insoluble in methanol.
- the obtained polymer contained a methanol-soluble fraction, which amounted to 54% of the entire quantity of the polymer.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerization Catalysts (AREA)
Abstract
A methanol-insoluble homopolymer of an α-trifluoromethylacrylate, which has either an alkyl group or a fluorine-containing alkyl group in the ester radical, is formed at good yields in an organic aprotic solvent by using an alkali metal alkoxide, e.g. lithium t-butoxide, as anionic polymerization catalyst.
Description
This invention relates to a method of anionically homopolymerizing an α-trifluoromethylacrylate to obtain a methanol-insoluble polymer.
Fluorine-containing acrylic or methacrylic esters provide industrially important functional polymers. In view of some properties unique to fluorine-containing polymers, such as excellent resistance to chemicals, water- and oil-repelling property and suitably low indices of refraction, extensive studies have been conducted on the uses of fluorine-containing acrylic or methacrylic polymers as or in, for example, paint materials, textile oil, plastic optical materials for optical fibers and other elements of optical circuits, contact lenses, dental materials and resist materials. Some items have already been developed to the stage of practical applications. Polymers of this category are acquiring greater importance as the needs for new functional materials are increasing in various fields of advanced technology.
At an earlier stage of the development, the aforementioned polymers were mostly of fluorine-containing acrylic or methacrylic esters represented by the general formula (A): ##STR1## wherein R is hydrogen atom or methyl group and R' is a fluorinated alkyl group. That is, fluorine atoms were introduced exclusively into the ester radical part of the monomer.
Recently, much studies have been made on polymerization of another group of fluorine-containing acrylic or methacrylic esters in which at least one fluorine atom is present in the α-position. For example, methyl α-fluoroacrylate can be homopolymerized at good yields by using a radical polymerization initiator, and can also be copolymerized with methyl methacrylate. (C. U. Pittman Jr. et al., Macromolecules, 13, 1031(1980)). Contrastively it is also known that methyl α-trifluoromethylacrylate cannot be homopolymerized by using an ordinary radical polymerization initiator though this compound can be homopolymerized by anionic polymerization using either n-butyllithium or pyridine as Catalyst. (H. Ito et al., Macromolecules, 15, 915(1982)). Some possibilites of radical copolymerization of the same compound with, e.g., methyl methacrylate are also reported. (H. Ito et al., Macromolecules, 17, 2204(1984)).
Thus, α-trifluoromethylacrylates are somewhat different in polymerizability from other fluorine-containing acrylic and methacrylic esters. Particularly, homopolymerization of an α-trifluoromethylacrylate can be accomplished only by anionic polymerization, and the yield of the homopolymer is very low when a popular anionic polymerization catalyst such as n-butyllithium or Grignard reagent is used. Although the yield of the polymer is improved to some extent by using pyridine as the catalyst, the obtained polymer consists of a methanol-soluble fraction and a methanol-insuluble fraction. That is, there is no industrially practicable method for anionic homopolymerization of α-trifluoromethylacrylates.
It is an object of the present invention to provide a method of preparing a homopolymer of an α-trifluoromethylacrylate, by which method an entirely methanol-insoluble polymer can be obtained with good yields.
We have succeeded in accomplishing the above object by discovering that many kinds of alkali metal alkoxides are highly effective as anionic polymerization catalyst for homopolymerization of α-trifluoromethylacrylates.
More definitely, this invention provides a method of preparing a homopolymer of an α-trifluoromethylacrylate represented by the general formula (1), the method comprising the step of keeping the monomer of the α-trifluoromethylacrylate dissolved in an organic solvent in the presence of an anionic polymerization catalyst which is an alkoxide represented by the general formula (2): ##STR2## wherein R represents an alkyl group or a fluorine-containing alkyl group:
R'OM (2)
wherein R' represents an alkyl group and M represents an alkali metal.
In the alkoxide the alkali metal M may be any of Li, Na, K, Rb and Cs. In practice, however, it is suitable to make a selection among lithium, sodium and potassium alkoxides, and it is preferable that the alkyl group R' in the alkoxide has from 1 to 4 carbon atom(s).
As will be understood from the general formula (1), the α-trifluoromethylacrylate monomer may contain fluorine atom(s) in the ester radical too. An example of such cases is 2,2,2-trifluoroethyl α-trifluoromethylacrylate.
The anionic homopolymerization according to the invention is carried out in the manner of solution polymerization. Depending on the combination of an α-trifluoromethylacrylate monomer and an organic solvent, the polymer may or may not dissolve in the solvent. Where the polymer dissolves in the solvent used for the polymerization reaction, the solution after the reaction is poured into a suitable liquid to cause complete precipitation of the polymer. In any case the anionic polymerization reaction must be performed in the absence of water and elemental or molecular oxygen. The polymerization reaction temperature is variable over the range of from about -78° C. to about 100° C. depending on the reaction materials.
In most cases homopolymers of α-trifluoromethylacrylates obtained by the method according to the invention are insoluble in methanol. These polymers are promising as high functional resins useful in various fields including paint materials. resist materials and plastic optical materials.
α-Trifluoromethylacrylates that can be homopolymerized by the method according to the invention include esters of α-trifluoromethylacrylic acid with an aliphatic alcohol, such as methyl α-trifluoromethyl acrylate, ethyl α-trifluoromethylacrylate, n-propyl α-trifluoromethylacrylate, isopropyl α-trifluoromethylacrylate, n-butyl α-trifluoromethylacrylate, t-butyl α-trifluoromethylacrylate and 2-ethylhexyl α-trifluoromethylacrylate, and esters of α-trifluoromethylacrylic acid with a fluorinated alcohol, such as 2,2,2-trifluoroethyl α-trifluoromethylacrylate, 1H,1H-heptafluorobutyl α-trifluoromethylacrylate, 1H,1H,7H-dodecafluoroheptyl α-trifluoromethylacrylate, 1H,1H-pentadecafluorooctyl α-trifluoromethylacrylate, 1H,1H-pentafluoropropyl α-trifluoromethylacrylate, 1H,1H-heptafluorobutyl α-trifluoromethylacrylate and hexafluoroisopropyl α-trifluoromethylacrylate.
Extremely high purity is not required of α-trifluoromethylacrylate monomers for use in this invention. In general, purity of 98% by gas chromatography is sufficient as far as the monomers are free of such impurities as will be obstructive to anionic polymerization reactions. Sufficient refining of each α-trifluoromethylacrylate monomer can be accomplished by simple distillation or by distillation in a nitrogen or helium gas stream in the presence of a suitable dehydrating agent such as calcium hydride.
The anionic polymerization reaction according to the invention must be carried out in an organic solvent which is practically free of water and elemental or molecular oxygen. It is suitable to use an inactive aprotic solvent which can be selected from aliphatic and aromatic hydrocarbons such as n-hexane, n-heptane, benzene, toluene and xylene and also from some ethers such as ethyl ether, di-n-butyl ether, tetrahydrofuran and dioxane. The selected solvent is dehydrated, degassed and refined by distillation. The quantity of the solvent per unit quantity of the reactant is not strictly limited.
An alkali metal alkoxide is chosen as the anionic polymerization catalyst. Typical examples of useful alkali metal alkoxides are lithium methoxide, sodium methoxide, potassium methoxide, lithium ethoxide, sodium ethoxide, potassium ethoxide, lithium n-propoxide. sodium n-propoxide, potassium n-propoxide, lithium isopropoxide, sodium isopropoxide, potassium isopropoxide, lithium n-butoxide, sodium n-butoxide, potassium n-butoxide, lithium t-butoxide, sodium t-butoxide and potassium t-butoxide. In most cases use of either lithium t-butoxide or potassium t-butoxide is preferable. The amount of the anionic polymerization catalyst is not necessarily limited. However, it is preferable that the catalyst amounts to 0.01-5 mol % of the α-trifluoromethylacrylate monomer.
The reactor to carry out the polymerization reaction may be of any type. For example, either an ampule-like glass reactor or an ordinary solution polymerization reactor provided with a stirrer can be used. It is necessary to dry out the interior of the reactor and to purge oxygen-containing gases from the reactor before charging the reaction materials into the reactor.
The reaction temperature for the polymerization ranges from about -78° C. to about 100° C. In general a very Suitable reaction temperature can be found within the range from -50° C. to 80° C.
After separating the polymer formed by a reaction according to the invention from the mother liquor or from the liquid used for precipitation, the polymer is washed first with dilute hydrochloric acid and then with water, followed by drying.
The invention will further be illustrated by the following nonlimitative examples.
Ethyl α-trifluoromethylacrylate monomer (b.p. 103°-105° C.) was refined by reflux distillation in the presence of calcium hydride. Together with 50 ml of toluene and 0.08 g (0.001 mol) of lithium t-butoxide, 8.4 g (0.05 mol) of refined ethyl α-trifluoromethylacrylate monomer was put into a glass ampule. After replacing the gas atmosphere in the ampule by nitrogen gas, the ampule was sealed and was left standing at -20° C. for 7 days to allow polymerization of the α-fluoromethylacrylate. The obtained polymer was washed first with dilute hydrochloric acid and then with water, and was dried under vacuum. The yield of the polymer was 100%.
In the infrared absorption spectrum of the obtained polymer, an absorption characteristic of C═O was observed at 1740 cm-1 and absorptions characteristic of CF3 at 1290, 1180 and 1100 cm-1. 1 H NMR measurement of the polymer dissolved in deuterated chloroform indicated the following peaks (from TMS): --CH2 CH3 1.3 ppm, --CH2 CH3 4.2 ppm, --CH2 2.6 ppm.
The polymer was insoluble in methanol, but it was soluble in any of tetrahydrofuran, chloroform and benzene.
Polymerization of ethyl α-trifluoromethylacrylate was carried out in accordance with Example 1 except that the reaction temperature was raised to 0° C. In this case the yield of the polymer was 61.5%.
Infrared absorption analysis and 1 H NMR measurement of the polymer gave the same results as in Example 1. Solubilities of this polymer in organic solvents did not differ from the solubilities of the polymer obtained in Example 1.
Polymerization of ethyl α-trifluoromethylacrylate was carried out in accordance with Example 1 except that 50 ml of tetrahydrofuran was used in place of toluene in Example 1 and that the reaction temperature was raised to 80° C. In this case the yield of the polymer was 58%.
Infrared absorption analysis and 1 H NMR measurement of the polymer gave the same results as in Example 1. Solubilities of this polymer in organic solvents did not differ from the solubilities of the polymer obtained in Example 1.
Using the same method and apparatus as in Example 1, 8.4 g (0.05 mol) of ethyl α-trifluoromethylacrylate was mixed with 50 ml of tetrahydrofuran and 0.112 g (0.001 mol) of potassium t-butoxide and was subjected to polymerization at -20° C. for 7 days. In this case the yield of the polymer was 60%.
Infrared absorption analysis and 1 H NMR measurement of the polymer gave the same results as in Example 1, and the solubilities of the polymer in organic solvents were the same as in the foregoing examples.
Using the same method and apparatus as in Example 1, 12.3 g (0.05 mol) of 2,2,2-trifluoroethyl α-trifluoromethylacrylate was mixed with 50 ml of toluene and 0.08 g (0.001 mol) of lithium t-butoxide and was subjected to polymerization at -20° C. for 7 days. The yield of the polymer was 83%. This polymer was insoluble in methanol.
Using the same method and apparatus as in Example 1, 14.5 g (0.05 mol) of hexafluoroisopropyl α-trifluoromethylacrylate was mixed with 50 ml of toluene and 0.08 g (0.001 mol) of lithium t-butoxide and was subjected to polymerization at -20° C. for 7 days. The yield of the polymer was 68%. This polymer was insoluble in methanol.
Together with 50 ml of toluene and 0.18 g (0.001 mol) of phenylmagnesium bromide. 8.4 g of refined ethyl α-trifluoromethylacrylate was put into a glass ampule. After replacing the gas atmosphere in the ampule by nitrogen gas, the ampule was sealed and was left standing at 0° C. for 7 days.
In this case, only 2% of the initial quantity of ethyl α-trifluoromethylacrylate polymerized.
Polymerization of ethyl α-trifluoromethylacrylate was tried by the same method as in Comparative Example 1 except that 0.064 g (0.001 mol) of n-butyllithium was used in place of phenylmagnesium bromide in Comparative Example 1 and that the reaction temperature was lowered to -20° C. As the result, only 3% of the initial quantity of ethyl α-trifluoromethylacrylate polymerized.
Using the same method and apparatus as in Comparative Example 1, 14.5 g (0.05 mol) of hexafluoroisopropyl α-trifluoromethylacrylate was mixed with 50 ml of toluene and 0.079 g (0.001 mol) of pyridine and was subjected to polymerization at 20° C. for 7 days. In this case the yield of the polymer was 56%.
The obtained polymer contained a methanol-soluble fraction, which amounted to 54% of the entire quantity of the polymer.
Claims (10)
1. A method of preparing a homopolymer of an α-trifluoromethylacrylate represented by the general formula (1). comprising the step of keeping the monomer of said α-trifluoromethylacrylate dissolved in an organic solvent in the presence of an anionic polymerization catalyst which is an alkoxide represented by the general formula (2): ##STR3## wherein R represents an alkyl group or a fluorine-containing alkyl group:
R'OM (2)
wherein R' represents an alkyl group and M represents an alkali metal.
2. A method according to claim 1, wherein R' in the general formula (2) represents an alkyl group having not more than 4 carbon atoms, and M in the general formula (2) represents Li, Na or K.
3. A method according to claim 1, wherein said alkoxide is selected from the group consisting of lithium t-butoxide and potassium t-butoxide.
4. A method according to claim 1, wherein said anionic polymerization catalyst amounts to 0.01-5 mol % of said monomer of said α-trifluoromethylacrylate.
5. A method according to claim 1, wherein said α-trifluoromethylacrylate is selected from the group consisting of methyl α-trifluoromethylacrylate, ethyl α-trifluoromethylacrylate, n-propyl α-trifluoromethylacrylate, isopropyl α-trifluoromethylacrylate, n-butyl α-trifluoromethylacrylate, t-butyl α-trifluoromethylacrylate and 2-ethylhexyl α-trifluoromethylacrylate.
6. A method according to claim 1, wherein said α-trifluoromethylacrylate is selected from the group consisting of 2,2,2-trifluoroethyl α-trifluoromethylacrylate, 1H,1H-heptafluorobutyl α-trifluoromethylacrylate, 1H,1H,7H-dodecafluoroheptyl α-trifluoromethylacrylate, 1H,1H-pentadecafluorooctyl α-trifluoromethylacrylate, 1H,1H-pentafluoropropyl α-trifluoromethylacrylate, 1H,1H-heptafluorobutyl α-trifluoromethylacrylate and hexafluoroisopropyl α-trifluoromethylacrylate.
7. A method according to claim 1, wherein said organic solvent is an aprotic solvent.
8. A method according to claim 7, wherein said organic solvent is selected from the group consisting of n-hexane, n-heptane, benzene, toluene, xylene, ethyl ether, di-n-butyl ether, tetrahydrofuran and dioxane.
9. A method according to claim 1, wherein the reaction system comprised of said monomer, said organic solvent and said anionic polymerization catalyst is kept at a temperature in the range from about -78° C. to about 100° C.
10. A method according to claim 9, wherein said temperature is in the range from -50° C. to 80° C.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60030623A JPS61190511A (en) | 1985-02-20 | 1985-02-20 | Production of fluorine-contained polymer |
| JP60-30623 | 1985-02-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4613657A true US4613657A (en) | 1986-09-23 |
Family
ID=12308982
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/826,585 Expired - Fee Related US4613657A (en) | 1985-02-20 | 1986-02-06 | Method for anionic homopolymerization of α-trifluoromethylacrylate |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US4613657A (en) |
| JP (1) | JPS61190511A (en) |
| DE (1) | DE3605515A1 (en) |
| FR (1) | FR2577559B1 (en) |
| GB (1) | GB2171708B (en) |
| IT (1) | IT1204345B (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4833207A (en) * | 1986-12-18 | 1989-05-23 | Kansai Paint Company, Limited | Curable compositions |
| US4863236A (en) * | 1986-03-06 | 1989-09-05 | Hoechst Aktiengesellschaft | Optical waveguide with an essentially fluorine-free polymer core and a fluorine-containing polymer jacket |
| WO1993023773A1 (en) * | 1992-05-14 | 1993-11-25 | Ciba-Geigy Ag | Process for preparation of oxygen permeable polymer material |
| US20030236369A1 (en) * | 2000-12-28 | 2003-12-25 | Central Glass Company, Limited | Transparent fluorine-containing copolymer |
| US6683202B2 (en) | 2001-02-22 | 2004-01-27 | Tokyo Ohka, Kogyo Co., Ltd. | Fluorine-containing monomeric ester compound for base resin in photoresist composition |
| US6710148B2 (en) | 2001-02-09 | 2004-03-23 | Shin Etsu Chemical Co., Ltd. | Polymers, resist compositions and patterning process |
| US6730451B2 (en) * | 1999-12-15 | 2004-05-04 | Shin-Etsu Chemical Co., Ltd. | Polymers, chemical amplification resist compositions and patterning process |
| US6835524B2 (en) * | 2000-02-16 | 2004-12-28 | Shin-Etsu Chemical Co., Ltd. | Polymers, chemical amplification resist compositions and patterning process |
| US20050058940A1 (en) * | 1998-10-27 | 2005-03-17 | Schadt Frank Leonard | Photoresists and processes for microlithography |
| US9709891B2 (en) | 2005-12-09 | 2017-07-18 | Fujifilm Corporation | Positive resist composition, resin used for the positive resist composition, compound used for synthesis of the resin and pattern forming method using the positive resist composition |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61120275A (en) * | 1984-11-16 | 1986-06-07 | Toshiba Corp | Japanese word processor |
| GB2199680A (en) * | 1986-11-28 | 1988-07-13 | Sharp Kk | Translating apparatus |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2472811A (en) * | 1946-04-27 | 1949-06-14 | Eastman Kodak Co | Polymers of alpha-fluoromethyl acrylic acid esters |
| US3285894A (en) * | 1963-10-11 | 1966-11-15 | Ceskoslovenska Akademie Ved | Polymerization initiators comprising alkali metal alcoholates |
| US3386977A (en) * | 1965-08-13 | 1968-06-04 | Geigy Chem Corp | Copolymers of perfuloroalkyl alpha-trifluoromethacrylates |
| US3422081A (en) * | 1965-11-15 | 1969-01-14 | Continental Can Co | Process for preparing stereoregular acrylamide polymers with an alkali metal alkoxide and polyvalent metal salt catalyst |
| US3457247A (en) * | 1965-02-12 | 1969-07-22 | Daikin Ind Ltd | Fluorocarbon compounds and polymers thereof |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL298889A (en) * | 1962-10-08 | 1965-08-10 | ||
| US4059616A (en) * | 1971-04-23 | 1977-11-22 | Rohm And Haas Company | Novel methacrylic polymers having allyl functionality |
| US4357435A (en) * | 1971-04-23 | 1982-11-02 | Rohm And Haas Company | Novel polymers of alkyl methacrylates |
-
1985
- 1985-02-20 JP JP60030623A patent/JPS61190511A/en active Granted
-
1986
- 1986-02-06 US US06/826,585 patent/US4613657A/en not_active Expired - Fee Related
- 1986-02-12 IT IT19378/86A patent/IT1204345B/en active
- 1986-02-14 GB GB08603637A patent/GB2171708B/en not_active Expired
- 1986-02-19 FR FR8602265A patent/FR2577559B1/en not_active Expired
- 1986-02-20 DE DE19863605515 patent/DE3605515A1/en active Granted
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2472811A (en) * | 1946-04-27 | 1949-06-14 | Eastman Kodak Co | Polymers of alpha-fluoromethyl acrylic acid esters |
| US3285894A (en) * | 1963-10-11 | 1966-11-15 | Ceskoslovenska Akademie Ved | Polymerization initiators comprising alkali metal alcoholates |
| US3457247A (en) * | 1965-02-12 | 1969-07-22 | Daikin Ind Ltd | Fluorocarbon compounds and polymers thereof |
| US3386977A (en) * | 1965-08-13 | 1968-06-04 | Geigy Chem Corp | Copolymers of perfuloroalkyl alpha-trifluoromethacrylates |
| US3422081A (en) * | 1965-11-15 | 1969-01-14 | Continental Can Co | Process for preparing stereoregular acrylamide polymers with an alkali metal alkoxide and polyvalent metal salt catalyst |
Non-Patent Citations (6)
| Title |
|---|
| C. U. Pittman, Jr. et al., Macromolecules 13, pp. 1031 1036 (1980). * |
| C. U. Pittman, Jr. et al., Macromolecules 13, pp. 1031-1036 (1980). |
| H. Ito et al, Macromolecules, 15, pp. 915 920 (1982). * |
| H. Ito et al, Macromolecules, 15, pp. 915-920 (1982). |
| H. Ito et al., Macromolecules 17, pp. 2204 2205 (1984). * |
| H. Ito et al., Macromolecules 17, pp. 2204-2205 (1984). |
Cited By (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4863236A (en) * | 1986-03-06 | 1989-09-05 | Hoechst Aktiengesellschaft | Optical waveguide with an essentially fluorine-free polymer core and a fluorine-containing polymer jacket |
| US4833207A (en) * | 1986-12-18 | 1989-05-23 | Kansai Paint Company, Limited | Curable compositions |
| WO1993023773A1 (en) * | 1992-05-14 | 1993-11-25 | Ciba-Geigy Ag | Process for preparation of oxygen permeable polymer material |
| US20050058940A1 (en) * | 1998-10-27 | 2005-03-17 | Schadt Frank Leonard | Photoresists and processes for microlithography |
| US7261993B2 (en) | 1998-10-27 | 2007-08-28 | E.I. Du Pont De Nemours And Company | Photoresists and processes for microlithography |
| US6884562B1 (en) * | 1998-10-27 | 2005-04-26 | E. I. Du Pont De Nemours And Company | Photoresists and processes for microlithography |
| US6730451B2 (en) * | 1999-12-15 | 2004-05-04 | Shin-Etsu Chemical Co., Ltd. | Polymers, chemical amplification resist compositions and patterning process |
| KR100592010B1 (en) * | 2000-02-16 | 2006-06-22 | 신에쓰 가가꾸 고교 가부시끼가이샤 | Polymer compound, chemically amplified resist material and pattern formation method |
| US6835524B2 (en) * | 2000-02-16 | 2004-12-28 | Shin-Etsu Chemical Co., Ltd. | Polymers, chemical amplification resist compositions and patterning process |
| US20060063902A1 (en) * | 2000-12-28 | 2006-03-23 | Central Glass Co., Ltd. | Transparent fluorine-containing copolymer |
| US7060771B2 (en) | 2000-12-28 | 2006-06-13 | Central Glass Company, Limited | Transparent fluorine-containing copolymer |
| US20030236369A1 (en) * | 2000-12-28 | 2003-12-25 | Central Glass Company, Limited | Transparent fluorine-containing copolymer |
| US7417100B2 (en) | 2000-12-28 | 2008-08-26 | Central Glass Company, Limited | Transparent fluorine-containing copolymer |
| US6710148B2 (en) | 2001-02-09 | 2004-03-23 | Shin Etsu Chemical Co., Ltd. | Polymers, resist compositions and patterning process |
| US6846949B2 (en) | 2001-02-22 | 2005-01-25 | Tokyo Ohka Kogyo Co., Ltd. | Fluorine-containing monomeric ester compound for base resin in photoresist composition |
| US20040122255A1 (en) * | 2001-02-22 | 2004-06-24 | Toshiyuki Ogata | Novel fluorine-containing monomeric ester compound for base resin in photoresist composition |
| US6683202B2 (en) | 2001-02-22 | 2004-01-27 | Tokyo Ohka, Kogyo Co., Ltd. | Fluorine-containing monomeric ester compound for base resin in photoresist composition |
| US9709891B2 (en) | 2005-12-09 | 2017-07-18 | Fujifilm Corporation | Positive resist composition, resin used for the positive resist composition, compound used for synthesis of the resin and pattern forming method using the positive resist composition |
| EP1795960B1 (en) * | 2005-12-09 | 2019-06-05 | Fujifilm Corporation | Positive resist composition, pattern forming method using the positive resist composition, use of the positive resit composition |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2577559A1 (en) | 1986-08-22 |
| GB8603637D0 (en) | 1986-03-19 |
| GB2171708B (en) | 1988-12-29 |
| JPH0419247B2 (en) | 1992-03-30 |
| IT1204345B (en) | 1989-03-01 |
| DE3605515C2 (en) | 1988-08-18 |
| FR2577559B1 (en) | 1988-07-01 |
| IT8619378A0 (en) | 1986-02-12 |
| DE3605515A1 (en) | 1986-08-21 |
| JPS61190511A (en) | 1986-08-25 |
| GB2171708A (en) | 1986-09-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4613657A (en) | Method for anionic homopolymerization of α-trifluoromethylacrylate | |
| JP2001122828A (en) | Bifunctional (meth)acrylic ester composition and dihydric alcohol therefor | |
| CA1290176C (en) | Optical waveguide with a core-jacket structure | |
| JPH0761980B2 (en) | Adamantyl mono (meth) acrylate derivative | |
| Yuki et al. | Stereospecific Polymerization of Methyl α-Phenylacrylate | |
| US5483005A (en) | Preparation of polymers with NLO-active side groups and the use thereof | |
| AU757140B2 (en) | Brominated materials | |
| US4578508A (en) | Fluoroacrylate ester, polymer thereof, and process of making the same | |
| EP0364587B1 (en) | Hexafluoroneopentyl alcohol, its derivatives, fluorinated polymers and their use | |
| US5198925A (en) | α-fluoroacrylic acid esters and polymers thereof | |
| Jariwala et al. | New hydrophobic and liquid-crystalline fluoroalkyl ether derivatives of ethyl α-(hydroxymethyl) acrylate: monomer synthesis and polymerization | |
| CA1280118C (en) | 1 .alpha.-FLUOROACRYLIC ACID ESTERS AND POLYMERS THEREOF | |
| US5319131A (en) | α-fluoroacrylic acid esters and polymers thereof | |
| JPS6322205B2 (en) | ||
| US5032654A (en) | Transparent polymer material | |
| US4633023A (en) | Fluoroacrylate ester, polymer thereof, and process of making the same | |
| JPS60170606A (en) | Preparation of fluorine-containing polymer | |
| US4841005A (en) | Tricyclodecane derivative | |
| CN110540610B (en) | (methyl) acrylate polymer and preparation method thereof | |
| JPH03127771A (en) | Thiocarboxylic acid ester compound and preparation thereof | |
| JP2923316B2 (en) | Adamantyl dicrotonate derivative | |
| CN100376606C (en) | Heavy-hydrogenated norbornyl (meth)acrylates, process for producing them, polymers thereof and optical members | |
| Gupta et al. | Polyacrylates containing hexafluoroisopropoxy pendant functions | |
| CN88101255A (en) | Transparent thermoplastic composition | |
| JPH0339304A (en) | Adamantyl monocrotonate-based polymer |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: CENTRAL GLASS COMPANY, LIMITED, NO. 5253, OAZA OKI Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNORS:NARITA, TADASHI;HAGIWARA, TOKIO;HAMANA, HIROSHI;REEL/FRAME:004514/0730 Effective date: 19860120 |
|
| FPAY | Fee payment |
Year of fee payment: 4 |
|
| REMI | Maintenance fee reminder mailed | ||
| LAPS | Lapse for failure to pay maintenance fees | ||
| FP | Lapsed due to failure to pay maintenance fee |
Effective date: 19940928 |
|
| STCH | Information on status: patent discontinuation |
Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362 |